Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Neosteo

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories3
Latest FDA decision2022-02-11
TypeNumberDevice NameCodeDateActions
510(k) K212545 FlexitSystem Knee osteotomy systemHRS2022-02-11 View
510(k) K192447 Superelastic StapleJDR2020-02-28 View
510(k) K191424 Interphalangeal Joint Fusion Device RangeHWC2019-08-28 View